Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197064666
- Species
- Rattus norvegicus
- Symbol
- rs197064666
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Cul5
- Location
- 8:54033572
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)8:54033572C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000099521.1:c.1158-1406G>A
- ENSEMBL:ENSRNOT00000114900.1:c.1404-1406G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:54012963...54066751 (53.79 kb)
- Assembly version
- Not Available
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